Tensor Surgical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3021286087
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3021286087
- Address
- 6345 S Pecos Rd Ste 212, Las Vegas, NV, 89120
Frequently asked questions
How many devices does TENSOR SURGICAL, INC. have in the registry?
The registry currently lists 2 devices for TENSOR SURGICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TENSOR SURGICAL, INC.'s devices?
Among its 2 most recently registered devices, TENSOR SURGICAL, INC. has devices listed in FDA GUDID (2 devices).
What risk classes do TENSOR SURGICAL, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for TENSOR SURGICAL, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from TENSOR SURGICAL, INC. in the registry?
The most recently registered devices listed for TENSOR SURGICAL, INC. include Tensor Surgical 3000 and Tensor Surgical VersaTip Suture Shuttle 4010.